U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Links from Gene

Items: 1 to 20 of 108

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7055630inversion1nstd229human GRCh38 chr5: 66,647,773-71,648,116 , GRCh37.p13 chr5: 65,943,601-70,943,943 OCLNP1, CDK7, 96 more genes
    nsv7046125inversion1nstd229human GRCh38 chr5: 69,199,477-71,010,577 , GRCh37.p13 chr5: 68,495,304-70,306,404 CDH12P3, LOC728488, 50 more genes
    nsv7045080inversion1nstd229human GRCh38 chr5: 67,733,468-69,446,994 , GRCh37.p13 chr5: 67,029,296-68,742,821 LOC105379013, KGD4, 31 more genes
    nsv6763618copy number variation1nstd229human GRCh38 chr5: 66,450,908-74,585,645 , GRCh37.p13 chr5: 65,746,736-73,881,470 LOC107986372, LOC105379027, 146 more genes
    nsv6313676copy number variation1nstd102humanPathogenic GRCh37 chr5: 64,049,692-70,306,646 , GRCh38.p12 chr5: 64,753,865-71,010,819 BCL9P1, CWC27, 105 more genes
    nsv6135434copy number variation1nstd213human GRCh37 chr5: 68,330,000-69,000,001 , GRCh38.p12 chr5: 69,034,173-69,704,174 , GRCh38.p12 chr5|NW_003315917.2: 1-337,557 CCNB1, CDK7, 26 more genes
    nsv6135416copy number variation1nstd213human GRCh37 chr5: 50,510,000-68,870,001 , GRCh38.p12 chr5: 51,214,166-69,574,174 , TRIM23, 243 more genes
    nsv5888268copy number variation1nstd209human GRCh38 chr5: 69,366,792-69,367,355 , GRCh37.p13 chr5: 68,662,619-68,663,182 RAD17, TAF9, 1 more genes
    nsv4593213copy number variation1nstd183human GRCh37 chr5: 68,664,883-68,667,150 , GRCh38.p12 chr5|NW_003315917.2: 152,252-154,519 , GRCh38.p12 chr5: 69,369,056-69,371,323 RAD17, TAF9, 1 more genes
    nsv4578696copy number variation1nstd102humanLikely pathogenic GRCh38 chr5: 58,780,641-73,523,380 , GRCh37.p13 chr5: 58,076,468-72,819,205 TRIM23, BTF3, 215 more genes
    nsv4495273mobile element insertion1nstd166human GRCh37.p13 chr5: 68,659,248-68,659,248 , GRCh38.p12 chr5|NW_003315917.2: 146,616-146,616 , GRCh38.p12 chr5: 69,363,421-69,363,421 TAF9, AK6
    nsv4436202copy number variation1nstd102humanUncertain significance GRCh37 chr5: 14,685,137-149,511,942 , GRCh38.p12 chr5: 14,685,028-150,132,379 RNU1-150P, RNU6-727P, 1757 more genes
    nsv3960535insertion1nstd168human GRCh38 chr5: 69,075,501-69,696,302 , GRCh37.p13 chr5: 68,371,328-68,992,129 CDK7, TAF9, 25 more genes
    nsv3921568copy number variation1nstd102humanPathogenic GRCh37 chr5: 64,228,590-68,791,331 , NCBI36 chr5: 64,264,346-68,827,087 , GRCh38 chr5: 64,932,763-69,495,504 LOC100419549, MAST4-AS1, 67 more genes
    nsv3920547copy number variation1nstd102humanUncertain significance GRCh38 chr5: 65,976,124-71,317,474 , NCBI36 chr5: 65,307,708-70,649,057 , GRCh37 chr5: 65,271,952-70,613,301 SMN1, NAIP, 97 more genes
    nsv3920421copy number variation1nstd102humanLikely pathogenic NCBI36 chr5: 62,538,695-70,622,774 , GRCh37 chr5: 62,502,939-70,587,018 , GRCh38 chr5: 63,207,112-71,291,191 TRIM23, CCNB1, 124 more genes
    nsv3912593copy number variation1nstd102humanUncertain significance NCBI36 chr5: 332,389-180,837,866 , GRCh37.p13 chr5: 279,389-180,905,260 , GRCh38.p12 chr5: 279,274-181,478,259 LOC105378993, LOC107986375, 2492 more genes
    nsv3911585copy number variation1nstd102humanPathogenic NCBI36 chr5: 75,149-73,744,306 , GRCh38 chr5: 22,149-74,412,725 , GRCh37 chr5: 22,149-73,708,550 LINC02241, ATPSCKMT, 878 more genes
    nsv3889848copy number variation1nstd102humanPathogenic GRCh37 chr5: 17,628,741-176,575,720 , GRCh38.p12 chr5: 17,628,632-177,148,719 MEGF10, LOC100128407, 2080 more genes
    nsv3886374copy number variation1nstd102humanPathogenic GRCh37 chr5: 13,648-180,905,029 , GRCh38.p12 chr5: 13,648-181,478,028 LOC105374618, HARS1, 2499 more genes
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Recent activity

    Clear Turn Off Turn On

    Your browsing activity is empty.

    Activity recording is turned off.

    Turn recording back on

    See more...
    You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)
    Support Center